Canonical Allele Identifier: CA1023900120
Gene: IL17RA HGNC NCBI

Linked Data

dbSNP Id: rs2061319956
gnomAD v3: 22-17084960-T-C
gnomAD v4: 22-17084960-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.17084960T>C , CM000684.2:g.17084960T>C GRCh38
NC_000022.10:g.17565850T>C , CM000684.1:g.17565850T>C GRCh37
NC_000022.9:g.15945850T>C NCBI36
NG_028257.1:g.5000T>C , LRG_355:g.5000T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000319363.10:c.-132T>C ENSP00000320936.6:n.-132T>C
ENST00000477874.1:n.7T>C
ENST00000612619.1:c.-132T>C ENSP00000479970.1:n.-132T>C
NM_001289905.1:c.-132T>C NP_001276834.1:n.-132T>C
NM_014339.6:c.-132T>C , LRG_355t1:c.-132T>C NP_055154.3:n.-132T>C
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